Katalyst CRO
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Sr. SAS Programmer
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Katalyst CRO . Responsibilities include: Supporting the Biostatistics team with programming activities and overseeing external vendors, ensuring timely and accurate programming and validation for clinical studies and publications. Contributing to the efficiency and best practices of the Biostatistics group, working effectively within a clinical team environment. Providing statistical programming and validation support for clinical study reports, coordinating activities among programmers, and overseeing external vendors when necessary. Developing and managing SDTM and ADaM datasets, statistical tables, figures, listings, and other data requests. Accessing and converting data from databases and file formats like MS Excel and text files. Collaborating with clinicians, statisticians, and publication managers to generate, QC, and review outputs and publications. Providing input for database and CRF development, creating edit check programs, and developing analysis plans and related documents. Maintaining programming standards and working independently to meet goals. Proposing improvements to programming processes. Requirements include: Bachelor's degree in a related science discipline. At least 7 years of SAS programming experience in a clinical trial setting. Proficiency in SAS-Base, MACRO, STAT, GRAPH, ACCESS, and MS Office. Experience with CDISC standards like SDTM and ADaM. Knowledge of Unix and Windows OS. Understanding of the software development lifecycle and FDA guidelines. Strong organizational, communication, and interpersonal skills, with the ability to work under pressure and meet deadlines. Additional details: Seniority level: Mid-Senior level Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is active and not expired. #J-18808-Ljbffr
Sr. SAS Programmer
role at
Katalyst CRO . Responsibilities include: Supporting the Biostatistics team with programming activities and overseeing external vendors, ensuring timely and accurate programming and validation for clinical studies and publications. Contributing to the efficiency and best practices of the Biostatistics group, working effectively within a clinical team environment. Providing statistical programming and validation support for clinical study reports, coordinating activities among programmers, and overseeing external vendors when necessary. Developing and managing SDTM and ADaM datasets, statistical tables, figures, listings, and other data requests. Accessing and converting data from databases and file formats like MS Excel and text files. Collaborating with clinicians, statisticians, and publication managers to generate, QC, and review outputs and publications. Providing input for database and CRF development, creating edit check programs, and developing analysis plans and related documents. Maintaining programming standards and working independently to meet goals. Proposing improvements to programming processes. Requirements include: Bachelor's degree in a related science discipline. At least 7 years of SAS programming experience in a clinical trial setting. Proficiency in SAS-Base, MACRO, STAT, GRAPH, ACCESS, and MS Office. Experience with CDISC standards like SDTM and ADaM. Knowledge of Unix and Windows OS. Understanding of the software development lifecycle and FDA guidelines. Strong organizational, communication, and interpersonal skills, with the ability to work under pressure and meet deadlines. Additional details: Seniority level: Mid-Senior level Employment type: Contract Job function: Information Technology Industry: Pharmaceutical Manufacturing This job posting is active and not expired. #J-18808-Ljbffr